4.6 Article

Mechanism of Vibrio cholerae Autoinducer-1 Biosynthesis

期刊

ACS CHEMICAL BIOLOGY
卷 6, 期 4, 页码 356-365

出版社

AMER CHEMICAL SOC
DOI: 10.1021/cb1003652

关键词

-

资金

  1. Howard Hughes Medical Institute
  2. National Institutes of Health (NIH) [5R01GM0-65859, 5R01AI054442, GM082061]
  3. National Science Foundation (NSF) [MCB-0343821]

向作者/读者索取更多资源

Vibrio cholerae, the causative agent of the disease cholera, uses a cell to cell communication process called quorum sensing to control biofilm formation and virulence factor production. The major V. cholerae quorum-sensing signal CAI-1 has been identified as (S)-3-hydroxytridecan-4-one, and the CqsA protein is required for CAI-1 production. However, the biosynthetic route to CAI-I remains unclear. Here we report that (S)-adenosylmethionine (SAM) is one of the two biosynthetic substrates for CqsA. CqsA couples SAM and decanoyl-coenzyme A to produce a previously unknown but potent quorum sensing molecule, 3-aminotridec-2-en-4-one (Ea-CAI-1). The CqsA mechanism is unique; it combines two enzymatic transformations, a beta,gamma-elimination of SAM and an acyltransferase reaction, into a single PLP-dependent catalytic process. Ea-CAI-1 is Subsequently converted to CAT 1, presumably through the intermediate tridecane-3,4-dione (DK-CAI-1). We propose that the Ea-CAI-1 to DK-CAI-1 conversion occurs spontaneously, and we identify the enzyme responsible for the subsequent step: conversion of DK-CAI-1 into CAI-1. SAM is the substrate for the synthesis of at least three different classes of quorum sensing signal molecules, indicating that bacteria have evolved a strategy to leverage an abundant substrate for multiple signaling purposes.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据